| TGA Action ID |
RC-2026-RN-00113-1 |
| Type of Product |
Medicine |
| Product Name/Description |
OXYCODONE SANDOZ - oxycodone hydrochloride 5 mg modified release tablet blister pack
Batch Number: PS9028
Expiry Date: 02/2028 |
| ARTG Number |
153605 |
| Action Type |
Product Alert |
| Action Level |
Retail |
| Hazard Classification |
Class II |
| Reason for the Action |
Sandoz has received reports that a batch of Oxycodone Sandoz Modified Release 5 mg tablets was supplied without the 'modified release' text on the blister back (foil text).
This may cause confusion between other forms of oxycodone, which could potentially lead to medication error. The carton (box) correctly describes the dosage form as modified release. |
| Instructions for Customers/Users |
Customers are to:
- Review the Customer Letter and be aware of the missing text on the blister back.
- Reassure patients and other related healthcare professionals that the product is modified-release and that this is clearly and correctly represented on the carton.
- Maintain best practice of storing medicines in their original packaging and encourage patients to do the same.
Product with corrected blister back is expected to be available from September 2026.
This action has been closed out on 12/05/2026 |
| Action Commencement Date |
16/02/2026 |
| Responsible Entity |
|
| Contact Information |
1800 726 369 - Sandoz Customer Service |